Fortrea

Job Overview:The Senior Marketing Manager Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies thought leadership and programs that advance business priorities and customer engagement. This role works closely with scientific clinical an

Job Overview:The Senior Marketing Manager Therapy Area Marketing supports the development and execution of therapyspecific marketing strategies thought leadership and programs that advance business priorities and customer engagement. This role works closely with scientific clinical an

Job Overview:The Database Associate II will provide technical services (Electronic Data Capture Remote Data Capture Oracle Clinical and Bedside Data Capture) on assigned projects to achieve project integrity and the delivery of on time quality data.Summary of Responsibilities:Perform

Job Overview:The Database Associate II will provide technical services (Electronic Data Capture Remote Data Capture Oracle Clinical and Bedside Data Capture) on assigned projects to achieve project integrity and the delivery of on time quality data.Summary of Responsibilities:Perform

Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical this position you will support the execution of clinical studies that contribute to improving global patient health and driving innovation in life sciences.Key ResponsibilitiesYou will c

Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical this position you will support the execution of clinical studies that contribute to improving global patient health and driving innovation in life sciences.Key ResponsibilitiesYou will c

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Summary of Responsibilities:Site management responsibility for clinical studies according to Fortreas Standard Operating Procedures ICH GCP Guidelines applicable project plans and Sponsor requirements including verification of study training records.Conducts site monitoring responsibi

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

Fortrea is excited to connect with talented individuals for future opportunities. If you meet the job requirements well invite you for an interview. If youre pre-selected our recruiter will keep in touch and let you know when the role officially opens so we can reconfirm your interest

*** Candidates with previous shipping and bio-hazard materials experience strongly preferred***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Lab Shipping Coordinator to in

*** Candidates with previous shipping and bio-hazard materials experience strongly preferred***As one of the largest Clinical Research Organizations in the world we have four Early Phase Clinical Research Units in the UK and US.We are currently seeking a Lab Shipping Coordinator to in

Job Overview:Manages and supports the study TMF right from the study set up to the closeout including the transfer of the TMF. Managing study TMF health and completeness. Responsible for initiating the Review workflow.Summary of Responsibilities:The position provides process control c

Job Overview:Manages and supports the study TMF right from the study set up to the closeout including the transfer of the TMF. Managing study TMF health and completeness. Responsible for initiating the Review workflow.Summary of Responsibilities:The position provides process control c

Bring Clinical Research to Life Join Us as a Site Navigator IAre you passionate about clinical research and enjoy working at the center of collaboration Were looking for a Site Navigator I to help guide investigative sites from feasibility to activation and ensure studies start stro

Bring Clinical Research to Life Join Us as a Site Navigator IAre you passionate about clinical research and enjoy working at the center of collaboration Were looking for a Site Navigator I to help guide investigative sites from feasibility to activation and ensure studies start stro

Job Overview:We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the matrix environ

Job Overview:We are seeking a highly skilled Workday PSA (Professional Services Automation) Architect to join our dynamic IT team. The ideal candidate will have extensive experience in Workday PSA and how to successfully deliver the solution within the challenges of the matrix environ

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

The Strategic Deals and Partnerships role will have global responsibility for driving strategic partnerships across biopharma accounts and other key organizations including financial entities supporting clinical trial funding. This position leads cross-functional Deal Teams to design

Summary of Responsibilities:Performs supervisory duties for Document Specialists (DSs) including but not limited to interviewing hiring training developing performance evaluation intervention discipline and discharge.Organizing gathering scanning and filing of all applicable documents

Summary of Responsibilities:Performs supervisory duties for Document Specialists (DSs) including but not limited to interviewing hiring training developing performance evaluation intervention discipline and discharge.Organizing gathering scanning and filing of all applicable documents

Job Overview:Responsible for general maintenance and any required archival of documents produced by the CPS Project Management Team. Organizing gathering scanning and filing of all applicable documents into appropriate electronic and/or paper copy locations including the Trial Master

Job Overview:Responsible for general maintenance and any required archival of documents produced by the CPS Project Management Team. Organizing gathering scanning and filing of all applicable documents into appropriate electronic and/or paper copy locations including the Trial Master

Come join Fortrea in a newly created HR Manager role embedded within our Dallas TX or Madison WI Clinical Research Units. This is a critical opportunity to partner closely with the teams delivering lifechanging research and to strengthen how we support develop and retain our people. S

Come join Fortrea in a newly created HR Manager role embedded within our Dallas TX or Madison WI Clinical Research Units. This is a critical opportunity to partner closely with the teams delivering lifechanging research and to strengthen how we support develop and retain our people. S

About the RoleAs a Senior Site Navigator youll act as a local country or regional expert in studystart-up leading site-level activities with minimal oversight. Youll be a trusted partner tosites and internal teams proactively identifying risks mentoring junior colleagues andensuring s

About the RoleAs a Senior Site Navigator youll act as a local country or regional expert in studystart-up leading site-level activities with minimal oversight. Youll be a trusted partner tosites and internal teams proactively identifying risks mentoring junior colleagues andensuring s

Fortrea is currently seeking anAssociate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-based position in Canada that

Fortrea is currently seeking anAssociate II (Patient Safety Solutions) to perform clinical trial and post approval adverse event case role requires strong clinical knowledge as well as an understanding of the US Healthcare system.This is a full-time home-based position in Canada that

Fortreas FSP team is hiring a Clinical Operation Manager- Finance - Hybrid in Montreal Canada. Must be bilingual in French & English. Job Overview:This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulat

Fortreas FSP team is hiring a Clinical Operation Manager- Finance - Hybrid in Montreal Canada. Must be bilingual in French & English. Job Overview:This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulat

Join Fortrea as a Senior Clinical Data Specialist within our Functional Service Provider (FSP) model where you will play a critical role in ensuring highquality clinical data that supports global drug development. This fully remote position offers the opportunity to contribute meaning

Join Fortrea as a Senior Clinical Data Specialist within our Functional Service Provider (FSP) model where you will play a critical role in ensuring highquality clinical data that supports global drug development. This fully remote position offers the opportunity to contribute meaning

We are currently seeking Sr CRAs with 4 years of monitoring within in United States. Travel is expected to be regional as well as to Puerto Rico (seeking a candidate with direct flight to PR) and about 50% overnight. Job Overview:The Senior CRA 2 is responsible for site monitoring and

We are currently seeking Sr CRAs with 4 years of monitoring within in United States. Travel is expected to be regional as well as to Puerto Rico (seeking a candidate with direct flight to PR) and about 50% overnight. Job Overview:The Senior CRA 2 is responsible for site monitoring and

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Provide medical safety expertise directly and indirectly to Sponsors of drugs devices and combination products in the post marketing period.Summary of Responsibilities:Undertake primary medical review of cases including medical assessment of the case for seriousness liste

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Demonstrate the ability to independently manage the production of safety deliverables including those involving complex data analyses or important saf

Job Overview:Lead the preparation and review of aggregate safety risk management signal detection and benefit-risk evaluation reports. Demonstrate the ability to independently manage the production of safety deliverables including those involving complex data analyses or important saf